Variant report

Variant	esv14835
Chromosome Location	chr4:78739915-78741153
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:78741127-78741751	K562	blood:	n/a	n/a
2	ATF2	chr4:78739303-78739934	GM12878	blood:	n/a	n/a
3	BACH1	chr4:78739516-78740668	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:78740390-78740590	K562	blood:	n/a	n/a
5	BCLAF1	chr4:78739679-78740049	GM12878	blood:	n/a	chr4:78739971-78739984
6	BCLAF1	chr4:78741000-78741946	GM12878	blood:	n/a	chr4:78741478-78741487 chr4:78741435-78741444 chr4:78741025-78741038 chr4:78741717-78741725 chr4:78741202-78741215 chr4:78741204-78741217 chr4:78741024-78741037
7	BCLAF1	chr4:78740969-78741793	GM12878	blood:	n/a	chr4:78741478-78741487 chr4:78741435-78741444 chr4:78741025-78741038 chr4:78741717-78741725 chr4:78741202-78741215 chr4:78741204-78741217 chr4:78741024-78741037
8	BCLAF1	chr4:78740282-78740756	GM12878	blood:	n/a	chr4:78740643-78740656 chr4:78740648-78740657
9	BCLAF1	chr4:78739244-78740197	GM12878	blood:	n/a	chr4:78740059-78740072 chr4:78739971-78739984 chr4:78740060-78740073
10	BHLHE40	chr4:78741151-78741656	HepG2	liver:	n/a	chr4:78741201-78741217 chr4:78741226-78741242 chr4:78741202-78741218
11	BHLHE40	chr4:78741125-78742120	K562	blood:	n/a	chr4:78741201-78741217 chr4:78741226-78741242 chr4:78741202-78741218
12	BHLHE40	chr4:78740971-78741973	GM12878	blood:	n/a	chr4:78741201-78741217 chr4:78741226-78741242 chr4:78741202-78741218
13	BHLHE40	chr4:78739220-78740500	K562	blood:	n/a	chr4:78740062-78740078
14	BHLHE40	chr4:78739767-78740169	HepG2	liver:	n/a	chr4:78740062-78740078
15	BHLHE40	chr4:78739710-78740704	GM12878	blood:	n/a	chr4:78740062-78740078
16	BRCA1	chr4:78739878-78739945	HepG2	liver:	n/a	n/a
17	BRCA1	chr4:78739990-78740013	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr4:78739324-78739968	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr4:78740986-78741771	K562	blood:	n/a	n/a
20	CCNT2	chr4:78739224-78741754	K562	blood:	n/a	chr4:78741442-78741451 chr4:78741506-78741515
21	CEBPB	chr4:78739319-78739929	Hela-S3	cervix:	n/a	n/a
22	CEBPD	chr4:78741125-78741778	HepG2	liver:	n/a	n/a
23	CEBPD	chr4:78740980-78741824	K562	blood:	n/a	n/a
24	CHD1	chr4:78740298-78740471	H1-hESC	embryonic stem cell:	n/a	chr4:78740328-78740338
25	CHD1	chr4:78741053-78741365	GM12878	blood:	n/a	n/a
26	CHD1	chr4:78738659-78742661	IMR90	lung:	n/a	chr4:78741736-78741746 chr4:78740328-78740338
27	CHD1	chr4:78739304-78740677	GM12878	blood:	n/a	chr4:78740328-78740338
28	CHD1	chr4:78739272-78739971	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr4:78740077-78740138	K562	blood:	n/a	n/a
30	CHD2	chr4:78741044-78741978	K562	blood:	n/a	chr4:78741736-78741746
31	CHD2	chr4:78741052-78741772	GM12878	blood:	n/a	chr4:78741736-78741746
32	CHD2	chr4:78740375-78740503	K562	blood:	n/a	n/a
33	CHD2	chr4:78739781-78739936	HepG2	liver:	n/a	n/a
34	CHD2	chr4:78739261-78741914	Hela-S3	cervix:	n/a	chr4:78741736-78741746 chr4:78740328-78740338
35	CHD2	chr4:78741143-78741593	HepG2	liver:	n/a	n/a
36	CHD2	chr4:78739752-78740589	GM12878	blood:	n/a	chr4:78740328-78740338
37	CHD2	chr4:78740314-78740317	HepG2	liver:	n/a	n/a
38	CREB1	chr4:78739676-78739947	A549	lung:	n/a	n/a
39	CREB1	chr4:78740994-78741880	GM12878	blood:	n/a	n/a
40	CREB1	chr4:78740911-78741990	HepG2	liver:	n/a	n/a
41	CREB1	chr4:78740932-78741936	K562	blood:	n/a	n/a
42	CREB1	chr4:78741079-78742043	K562	blood:	n/a	n/a
43	CTBP2	chr4:78741068-78741927	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTBP2	chr4:78739250-78740791	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr4:78739780-78739930	GM12867	blood:	n/a	n/a
46	CTCF	chr4:78739834-78739998	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:78741108-78741218	NHEK	skin:	n/a	n/a
48	CTCF	chr4:78740780-78740930	GM12867	blood:	n/a	n/a
49	CTCF	chr4:78739792-78739939	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:78741060-78741210	SK-N-SH_RA	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:78741143-78741193	HCF	heart:	n/a
2	chr4:78740080-78740130	NHDF-neo	bronchial:	n/a
3	chr4:78740080-78740130	AG04450	lung:	fetal
4	chr4:78740080-78740130	HCF	heart:	n/a
5	chr4:78740080-78740130	U87	brain:	n/a
6	chr4:78741143-78741193	SK-N-MC	brain:	n/a
7	chr4:78740310-78740360	HRCEpiC	kidney:	n/a
8	chr4:78741143-78741193	HepG2	liver:	n/a
9	chr4:78741143-78741193	HCT-116	colon:	n/a
10	chr4:78740080-78740130	HEK293	kidney:	embryo
11	chr4:78740310-78740360	AG10803	skin:	n/a
12	chr4:78740310-78740360	Caco-2	colon:	n/a
13	chr4:78741143-78741193	AG04449	skin:	fetal
14	chr4:78740080-78740130	NH-A	brain:	n/a
15	chr4:78740080-78740130	AG09319	gingival:	n/a
16	chr4:78741143-78741193	Jurkat	blood:	n/a
17	chr4:78741143-78741193	AG04450	lung:	fetal
18	chr4:78740310-78740360	GM12892	blood:	n/a
19	chr4:78740310-78740360	AG09309	skin:	n/a
20	chr4:78740080-78740130	MCF-7	breast:	n/a
21	chr4:78740310-78740360	AG04450	lung:	fetal
22	chr4:78740080-78740130	GM06990	blood:	n/a
23	chr4:78740080-78740130	HepG2	liver:	n/a
24	chr4:78740310-78740360	HUVEC	blood vessel:	n/a
25	chr4:78740080-78740130	RPTEC	kidney:	n/a
26	chr4:78740080-78740130	AoSMC	blood vessel:	n/a
27	chr4:78740080-78740130	LNCaP	prostate:	n/a
28	chr4:78741143-78741193	GM06990	blood:	n/a
29	chr4:78740080-78740130	PFSK-1	brain:	n/a
30	chr4:78740080-78740130	ovcar-3	ovarian:	n/a
31	chr4:78741143-78741193	HL-60	blood:	n/a
32	chr4:78741143-78741193	HNPCEpiC	eye:	n/a
33	chr4:78740080-78740130	GM12891	blood:	n/a
34	chr4:78740310-78740360	BE2_C	brain:	n/a
35	chr4:78740310-78740360	Hela-S3	cervix:	n/a
36	chr4:78740310-78740360	GM06990	blood:	n/a
37	chr4:78740080-78740130	NHBE	bronchial:	n/a
38	chr4:78740080-78740130	K562	blood:	n/a
39	chr4:78740080-78740130	A549	lung:	n/a
40	chr4:78741143-78741193	AG10803	skin:	n/a
41	chr4:78740080-78740130	Jurkat	blood:	n/a
42	chr4:78740310-78740360	NB4	blood:	n/a
43	chr4:78740310-78740360	PrEC	prostate:	n/a
44	chr4:78740310-78740360	HNPCEpiC	eye:	n/a
45	chr4:78740080-78740130	HMEC	breast:	n/a
46	chr4:78740080-78740130	SK-N-MC	brain:	n/a
47	chr4:78740080-78740130	AG09309	skin:	n/a
48	chr4:78741143-78741193	HMEC	breast:	n/a
49	chr4:78740080-78740130	AG04449	skin:	fetal
50	chr4:78741143-78741193	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:100998097..100998597-chr4:78741144..78741880,2	Hela-S3	cervix:
2	chr4:78740326..78742288-chr4:79472480..79474297,2	MCF-7	breast:
3	chr4:78740903..78742923-chr4:78749495..78752276,3	MCF-7	breast:
4	chr4:78734703..78743448-chr4:78779372..78785561,20	K562	blood:
5	chr4:78738764..78744926-chr4:78780904..78785516,9	MCF-7	breast:
6	chr4:78739289..78742998-chr4:78782109..78787360,12	MCF-7	breast:
7	chr4:78739575..78742806-chr4:78977392..78979889,3	MCF-7	breast:
8	chr4:78739409..78741307-chr4:83294294..83296166,2	MCF-7	breast:
9	chr4:78738995..78744410-chr4:78782336..78785612,12	K562	blood:
10	chr4:78739575..78741919-chr4:78878334..78880056,2	MCF-7	breast:

Variant related genes	Relation type
CNOT6L	TF binding region
CNOT6L	CpG island
ENSG00000169288	chromatin interactions
ENSG00000272677	chromatin interactions
ENSG00000138759	chromatin interactions
ENSG00000138772	chromatin interactions
ENSG00000248926	chromatin interactions
ENSG00000138668	chromatin interactions
ENSG00000250214	chromatin interactions

Extended variants
information (count: 52 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:52 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574206256	chr4:78739915-78739916	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs142405311	chr4:78739942-78739943	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs559836669	chr4:78739961-78739962	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs573259151	chr4:78739985-78739986	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs545450002	chr4:78740024-78740025	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs6811439	chr4:78740066-78740067	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs368945536	chr4:78740080-78740081	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs549963628	chr4:78740105-78740106	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs6828302	chr4:78740132-78740133	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs77103397	chr4:78740160-78740161	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs144725638	chr4:78740169-78740170	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs386676376	chr4:78740170-78740171	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs565860028	chr4:78740200-78740201	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs371841161	chr4:78740203-78740204	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs373313499	chr4:78740204-78740205	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs368900394	chr4:78740228-78740229	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs71214371	chr4:78740229-78740230	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs367722470	chr4:78740245-78740246	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs550976206	chr4:78740246-78740247	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs570967867	chr4:78740314-78740315	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs536752989	chr4:78740350-78740351	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs556827038	chr4:78740354-78740355	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs574167915	chr4:78740368-78740369	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs368783905	chr4:78740380-78740381	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs372837916	chr4:78740391-78740392	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs536480981	chr4:78740395-78740396	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs377011334	chr4:78740418-78740419	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs553611249	chr4:78740420-78740421	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs573604957	chr4:78740426-78740427	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs545388263	chr4:78740436-78740437	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs369622547	chr4:78740474-78740475	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs200614151	chr4:78740484-78740485	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs376150620	chr4:78740505-78740506	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs199615565	chr4:78740509-78740510	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs544681236	chr4:78740510-78740511	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs573178011	chr4:78740527-78740528	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs561257231	chr4:78740529-78740530	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs373050954	chr4:78740532-78740533	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs529061546	chr4:78740535-78740536	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs548926923	chr4:78740539-78740540	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs559564245	chr4:78740574-78740575	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs528377645	chr4:78740578-78740579	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs550914647	chr4:78740654-78740655	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs540511129	chr4:78740682-78740683	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs530465477	chr4:78740689-78740690	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs111723108	chr4:78740788-78740789	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs35410799	chr4:78740911-78740912	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs571445224	chr4:78740921-78740922	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs550635564	chr4:78740925-78740926	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs151238051	chr4:78741063-78741064	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:143 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78737000-78742400	Active TSS	Thymus	Thymus
2	chr4:78738600-78742000	Active TSS	Primary T cells fromperipheralblood	blood
3	chr4:78738600-78742000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr4:78738600-78742200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr4:78738600-78742200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr4:78738600-78742200	Active TSS	Fetal Intestine Small	intestine
7	chr4:78738600-78742200	Active TSS	Psoas Muscle	Psoas
8	chr4:78738600-78742200	Active TSS	NHLF	lung
9	chr4:78738600-78742600	Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr4:78738600-78742600	Active TSS	Right Atrium	heart
11	chr4:78738800-78742200	Active TSS	Sigmoid Colon	Sigmoid Colon
12	chr4:78738800-78742200	Active TSS	Small Intestine	intestine
13	chr4:78738800-78742400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr4:78738800-78742400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr4:78738800-78742400	Active TSS	Fetal Intestine Large	intestine
16	chr4:78738800-78742400	Active TSS	Fetal Muscle Trunk	muscle
17	chr4:78738800-78742400	Active TSS	Left Ventricle	heart
18	chr4:78738800-78742400	Active TSS	Pancreas	Pancrea
19	chr4:78738800-78742400	Active TSS	Right Ventricle	heart
20	chr4:78738800-78742800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
21	chr4:78739000-78741800	Active TSS	HMEC	breast
22	chr4:78739000-78742000	Active TSS	Primary T helper cells PMA-I stimulated	--
23	chr4:78739000-78742000	Active TSS	Fetal Thymus	thymus
24	chr4:78739000-78742000	Active TSS	Ovary	ovary
25	chr4:78739000-78742000	Active TSS	HSMM	muscle
26	chr4:78739000-78742200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr4:78739000-78742200	Active TSS	Rectal Mucosa Donor 29	rectum
28	chr4:78739000-78742400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr4:78739000-78742600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr4:78739000-78742600	Active TSS	Esophagus	oesophagus
31	chr4:78739000-78742800	Active TSS	Aorta	Aorta
32	chr4:78739200-78740200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
33	chr4:78739200-78740400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr4:78739200-78740600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
35	chr4:78739200-78741600	Active TSS	HSMMtube	muscle
36	chr4:78739200-78741800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr4:78739200-78741800	Active TSS	Fetal Muscle Leg	muscle
38	chr4:78739200-78741800	Active TSS	Gastric	stomach
39	chr4:78739200-78741800	Active TSS	Lung	lung
40	chr4:78739200-78741800	Active TSS	NHEK	skin
41	chr4:78739200-78742000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr4:78739200-78742000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr4:78739200-78742000	Active TSS	Breast Myoepithelial Primary Cells	Breast
44	chr4:78739200-78742000	Active TSS	Primary T cells from cord blood	blood
45	chr4:78739200-78742000	Active TSS	Primary T helper naive cells from peripheral blood	blood
46	chr4:78739200-78742000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
47	chr4:78739200-78742000	Active TSS	Brain Anterior Caudate	brain
48	chr4:78739200-78742000	Active TSS	Brain Cingulate Gyrus	brain
49	chr4:78739200-78742000	Active TSS	Brain Hippocampus Middle	brain
50	chr4:78739200-78742000	Active TSS	Duodenum Mucosa	Duodenum

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